Clinical Research Associate

JR United Kingdom; Chester; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading CRO is seeking a Freelance Clinical Research Associate (CRA) to join their team remotely in the UK. This position offers a competitive hourly rate and the flexibility to manage multiple clinical trials while ensuring compliance with regulations. Ideal candidates will have relevant experience in clinical trials and a strong understanding of GCP guidelines.

Benefits

Flexible schedule

Ongoing projects for long-term collaboration

Qualifications

• Minimum 2 years of recent CRA experience in the UK.
• Strong knowledge of GCP and FDA regulations required.
• Ability to work independently and manage multiple sites.

Responsibilities

• Monitor clinical trial sites and ensure compliance with protocols.
• Review site documentation for accuracy and completeness.
• Build strong relationships with site staff.

Skills

Understanding of GCP

Clinical trial processes

Strong communication skills

Education

Bachelor’s degree in life sciences or related field

Tools

EDC systems

Job description

Now Hiring: Freelance Clinical Research Associate (CRA) – Remote (UK-Based)

Contract | Competitive Hourly Rate | Flexible Schedule

I'm working with a growing, full-service CRO that’s looking to bring an experienced Freelance CRA on board to support upcoming clinical trials. This is a great opportunity for someone who enjoys working independently, values flexibility, and wants to be part of a collaborative team environment.

About the CRO:

This is a small but expanding CRO that partners with biotech and pharma companies on early- to late-phase clinical trials. They’re known for being responsive, thorough, and committed to quality. As their study portfolio grows, they’re adding freelance CRAs to their network who can jump in and take ownership of site monitoring activities.

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What You'll Be Doing:

• Monitor clinical trial sites across various stages—site selection, initiation, routine monitoring, and close-out
• Ensure sites are following protocol, GCP, and all applicable regulations
• Review source data, CRFs, and site documentation for accuracy and completeness
• Identify and follow up on any site issues or deviations
• Build strong working relationships with site staff
• Prepare and submit clear and timely visit reports
• Work closely with the internal clinical project team to keep things moving smoothly

What We're Looking For:

• At least 2 years of recent CRA experience in the U.k (independent or CRO-based)
• Strong understanding of GCP, FDA regulations, and clinical trial processes
• Background in life sciences, nursing, or a related field (Bachelor’s degree required)
• Able to work independently and manage multiple sites
• Comfortable with EDC systems and remote monitoring tools
• Based in the U.K. with ability to travel regionally as needed (up to ~60%)

Nice to Have:

• Experience with women's health, Neurology and Medical device
• Previous work with smaller CROs or sponsor teams
• A flexible, problem-solving approach

Why This Role?

• Competitive hourly pay
• Full remote flexibility + site travel
• Ongoing projects with potential for long-term collaboration
• A tight-knit team that values your input and expertise